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Joanna Madzio
Joanna Madzio
Medical University of Lodz
Zweryfikowany adres z umed.lodz.pl
Tytuł
Cytowane przez
Cytowane przez
Rok
Biallelic loss of CDKN2A is associated with poor response to treatment in pediatric acute lymphoblastic leukemia
M Braun, A Pastorczak, W Fendler, J Madzio, B Tomasik, J Taha, ...
Leukemia & lymphoma 58 (5), 1162-1171, 2017
512017
Neutrophil elastase defects in congenital neutropenia
Z Rydzynska, B Pawlik, D Krzyzanowski, W Mlynarski, J Madzio
Frontiers in Immunology 12, 653932, 2021
322021
Targeting the thioredoxin system as a novel strategy against B‐cell acute lymphoblastic leukemia
K Fidyt, A Pastorczak, A Goral, K Szczygiel, W Fendler, A Muchowicz, ...
Molecular Oncology 13 (5), 1180-1195, 2019
312019
Differential regulation of serum microRNA expression by HNF1β and HNF1α transcription factors
W Fendler, J Madzio, K Kozinski, K Patel, J Janikiewicz, M Szopa, A Tracz, ...
Diabetologia 59 (7), 1463-1473, 2016
232016
Surface expression of cytokine receptor-like factor 2 increases risk of relapse in pediatric acute lymphoblastic leukemia patients harboring IKZF1 deletions
A Pastorczak, L Sedek, M Braun, J Madzio, A Sonsala, M Twardoch, ...
Oncotarget 9 (40), 25971, 2018
172018
Prognostic significance of IKZF1 deletions and IKZF1plus profile in children with B‐cell precursor acute lymphoblastic leukemia treated according to the ALL‐IC …
M Braun, A Pastorczak, Ł Sędek, J Taha, J Madzio, I Jatczak‐Pawlik, ...
Hematological Oncology 40 (3), 430-441, 2022
142022
GATA3 germline variant is associated with CRLF2 expression and predicts outcome in pediatric B‐cell precursor acute lymphoblastic leukemia
J Madzio, A Pastorczak, L Sedek, M Braun, J Taha, K Wypyszczak, ...
Genes, Chromosomes and Cancer 58 (9), 619-626, 2019
122019
Potent, p53-independent induction of NOXA sensitizes MLL-rearranged B-cell acute lymphoblastic leukemia cells to venetoclax
K Fidyt, A Pastorczak, J Cyran, NT Crump, A Goral, J Madzio, ...
Oncogene 41 (11), 1600-1609, 2022
112022
Selected miRNA levels are associated with IKZF1 microdeletions in pediatric acute lymphoblastic leukemia
J Krzanowski, J Madzio, A Pastorczak, A Tracz, M Braun, J Tabarkiewicz, ...
Oncology Letters 14 (3), 3853-3861, 2017
112017
Genetic variability of GCKR alters lipid profiles in children with monogenic and autoimmune diabetes
A Tracz, J Madzio, P Gnys, B Malachowska, M Borowiec, K Wyka, ...
Experimental and Clinical Endocrinology & Diabetes, 503-509, 2014
62014
Heterozygous carriers of germline c. 657_661del5 founder mutation in NBN gene are at risk of central nervous system relapse of B-cell precursor acute lymphoblastic leukemia
B Tomasik, A Pastorczak, W Fendler, M Bartłomiejczyk, M Braun, M Mycko, ...
haematologica 103 (5), e200, 2018
52018
A high prevalence of neutrophil‐specific antibodies in ELANE‐mutated severe congenital neutropenia
W Dobrewa, J Madzio, K Babol‐Pokora, P Lopacz, A Gierszon, K Guz, ...
Pediatric Blood & Cancer 70 (4), e30247, 2023
42023
The kinetics of blast clearance are associated with copy number alterations in childhood B-cell acute lymphoblastic leukemia
Z Urbańska, M Lejman, J Taha, J Madzio, K Ostrowska, K Miarka-Walczyk, ...
Neoplasia 35, 100840, 2023
42023
Gene expression of ASNS, LGMN and CTSB is elevated in a subgroup of childhood BCP‑ALL with PAX5 deletion
E Wrona, J Jakubowska, B Pawlik, A Pastorczak, J Madzio, M Lejman, ...
Oncology letters 18 (6), 6926-6932, 2019
42019
The paradox of autoimmunity and autoinflammation in inherited neutrophil disorders–in search of common patterns
D Krzyzanowski, A Oszer, J Madzio, M Zdunek, J Kolodrubiec, B Urbanski, ...
Frontiers in Immunology 14, 1128581, 2023
22023
Molecular background and therapeutic perspectives of acute lymphoblastic leukemia BCR-ABL1-like
J Madzio, A Pastorczak, W Młynarski
Hematologia 5 (2), 154-161, 2014
22014
Elevated level of lysophosphatidic acid among patients with HNF1B mutations and its role in RCAD syndrome: a multiomic study
B Małachowska, J Janikiewicz, K Pietrowska, K Wyka, J Madzio, ...
Metabolomics 18 (3), 15, 2022
12022
Neutrophil functions in patients with neutropenia due to glycogen storage disease type 1b treated with empagliflozin
M Kaczor, S Malicki, J Folkert, E Dobosz, D Bryzek, B Chruścicka-Smaga, ...
Blood Advances, bloodadvances. 2023012403, 2024
2024
Concomitant inhibition of the thioredoxin system and nonhomologous DNA repair potently sensitizes Philadelphia‐positive lymphoid leukemia to tyrosine kinase inhibitors
L Komorowski, A Dabkowska, J Madzio, A Pastorczak, K Szczygiel, ...
HemaSphere 8 (3), e56, 2024
2024
CRISPR/Cas9 Strategy for Correcting ELANE Mutations and Restoring Neutrophil Differentiation in Severe Congenital Neutropenia: Insights from Patient-Derived iPSCs
Z Rydzynska, D Grzela, MI Linder, W Dobrewa, Z Urbanska, B Pawlik, ...
Blood 142, 4100, 2023
2023
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